Nordic Guidelines for Germline Predisposition to Myeloid Neoplasms in Adults: Recommendations for Genetic Diagnosis, Clinical Management and Follow-up

Panagiotis Baliakas(Uppsala University), Bianca Tesi(Karolinska University Hospital), Ulla Wartiovaara‐Kautto(Helsinki University Hospital), Asbjørg Stray‐Pedersen(Oslo University Hospital), Lone Smidstrup Friis(Copenhagen University Hospital), Ingunn Dybedal(Oslo University Hospital), Randi Hovland(Haukeland University Hospital), Kirsi Jahnukainen(Helsinki University Hospital), Klas Raaschou‐Jensen(Odense University Hospital), Per Ljungman(Karolinska University Hospital), Cecilie F. Rustad(Uppsala University), Charlotte Kvist Lautrup(Uppsala University), Outi Kilpivaara(Uppsala University), Astrid Olsnes Kittang(Uppsala University), Kirsten Grønbæk(Uppsala University), Jörg Cammenga(Uppsala University), Eva Hellström‐Lindberg(Uppsala University), Mette Klarskov Andersen(Uppsala University)
HemaSphere
November 22, 2019
Cited by 93Open Access
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Abstract

Myeloid neoplasms (MNs) with germline predisposition have recently been recognized as novel entities in the latest World Health Organization (WHO) classification for MNs. Individuals with MNs due to germline predisposition exhibit increased risk for the development of MNs, mainly acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). Setting the diagnosis of MN with germline predisposition is of crucial clinical significance since it may tailor therapy, dictate the selection of donor for allogeneic hematopoietic stem cell transplantation (allo-HSCT), determine the conditioning regimen, enable relevant prophylactic measures and early intervention or contribute to avoid unnecessary or even harmful medication. Finally, it allows for genetic counseling and follow-up of at-risk family members. Identification of these patients in the clinical setting is challenging, as there is no consensus due to lack of evidence regarding the criteria defining the patients who should be tested for these conditions. In addition, even in cases with a strong suspicion of a MN with germline predisposition, no standard diagnostic algorithm is available. We present the first version of the Nordic recommendations for diagnostics, surveillance and management including considerations for allo-HSCT for patients and carriers of a germline mutation predisposing to the development of MNs.


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